Trials / Unknown
UnknownNCT04200014
Bradycardia Risk Stratification With Loop Recorder After Syncope
Bradycardia High Risk Patient Identification After Syncope With Loop Recorder an Observational Study in Nancy University Hospital
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 250 (estimated)
- Sponsor
- Central Hospital, Nancy, France · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
Syncope is a common symptom that may be related to a conductive disorder. If no bradycardia is authenticated, it is often necessary to implant an implantable loop recorder. In somes cases, implantable loop recorder records cardiac conductive disorders. In this study, we want to try to identify a group of patients for whom we could immediately implant a pacemaker without prior implantation of an implantable loop recorder given the high probability of implantation of a pacemaker after interrogation of the implantable loop recorder. It would be interesting for the reduction of interventions for the patients and for the economic aspect of the healthcare system
Conditions
Timeline
- Start date
- 2019-12-09
- Primary completion
- 2020-01-31
- Completion
- 2020-03-31
- First posted
- 2019-12-16
- Last updated
- 2020-01-10
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT04200014. Inclusion in this directory is not an endorsement.